GPS Case Management Medical Review Therapeutic Area Leader

About the role

Lilly seeks a leader in Medical Review Supervision to oversee the safety evaluation of drugs and build expertise in the therapeutic area.

Responsibilities

• Supervise Case Management Medical Reviewers across the global team, including physicians and scientists.
• Develop and maintain technical expertise and medical knowledge in the therapeutic area.
• Lead process improvement and innovation projects to enhance safety evaluations.
• Manage resources to meet business objectives and future needs within the therapeutic area.
• Collaborate cross-functionally to align goals and deliverables, adjusting as needed.
• Partner with global GPS partners for efficient resource forecasting, planning, and utilization.
• Represent the role of safety in the organization and interact with key customers.
• Manage actions required to address safety issues in collaboration with global teams.
• Ensure compliance with the roles and responsibilities of the EU Qualified Person (QP).

Requirements

• BS degree in health-related or scientific field with 7 years of experience in pharmaceutical industry.
• Experience in clinical trial experience or areas relevant to drug discovery or development.
• Advanced medical related graduate degree, such as DVM, PharmD, PhD, MSN, or equivalent experience.
• Knowledge of drug development process.
• Fluent in English with excellent written and verbal communication skills.
• Strong clinical/diagnostic skills.
• Excellent interpersonal, organizational, and negotiation skills.
• Ability to work on multiple projects and function effectively in a fast-paced matrixed environment.
• Ability to prioritize tasks and shift priorities rapidly to meet tight deadlines.
• Ability to influence others (both cross-functionally and within the function) to create a positive working environment.
• Willingness to engage in domestic and international travel as necessary.

Qualifications

• Minimum of 7 years of experience in pharmaceutical industry, directly related clinical trial experience, or experience in areas relevant to drug discovery or development.
• Experience in the drug development process.

Skills

• Strong leadership and supervisory skills.
• Expertise in medical review and regulatory processes.
• Effective communication and collaboration abilities.
• Ability to manage resources and meet business objectives.
• Knowledge of drug development and pharmacovigilance.

Benefits

Eligible for a comprehensive benefit program including a company-sponsored 401(k), pension, vacation benefits, medical, dental, vision, and prescription drug benefits, flexible benefits, life insurance, death benefits, time off and leave of absence benefits, and well-being benefits.

Pay

$156,000 - $228,800

Schedule

Full-time equivalent employees are eligible for a company bonus (depending, in part, on company and individual performance).